Jump To Section:

Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References XML

Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2012-09-12 03:37:46 UTC

Update Date

2022-03-07 02:57:10 UTC

HMDB ID

HMDB0041711

Secondary Accession Numbers

HMDB41711

Metabolite Identification

Common Name

cis-Resveratrol 3-O-glucuronide

Description

cis-Resveratrol 3-O-glucuronide belongs to the class of organic compounds known as stilbene glycosides. Stilbene glycosides are compounds structurally characterized by the presence of a carbohydrate moiety glycosidically linked to the stilbene skeleton. cis-Resveratrol 3-O-glucuronide is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. Based on a literature review a small amount of articles have been published on cis-Resveratrol 3-O-glucuronide.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv0541 02271201282D          

 29 31  0  0  0  0            999 V2000
   -2.5377    0.7662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5377   -0.0588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2522   -0.4713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9667   -0.0588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9667    0.7662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2522    1.1787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2522    2.0037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9667    2.4162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6811   -0.4713    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8232   -0.4713    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6811    2.0037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3956    0.7662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1101    1.1787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1101    2.0037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3956    2.4162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6811    1.1787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8245    0.7662    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5377   -1.7088    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5377   -2.5338    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8232   -2.9463    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1087   -2.5338    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1088   -1.7088    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8232   -1.2963    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3943   -1.2963    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3943   -2.9463    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8232   -3.7713    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2522   -2.9463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2522   -3.7713    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9666   -2.5339    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  4  9  1  0  0  0  0
  2 10  1  0  0  0  0
  8 11  1  0  0  0  0
 15 11  2  0  0  0  0
 11 16  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 12 16  2  0  0  0  0
 13 17  1  0  0  0  0
 23 10  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 18 23  1  0  0  0  0
 22 24  1  6  0  0  0
 21 25  1  1  0  0  0
 20 26  1  6  0  0  0
 19 27  1  1  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
M  END

HMDB0041711
     RDKit          3D
cis-Resveratrol 3-O-glucuronide
 49 51  0  0  0  0  0  0  0  0999 V2000
   -3.3297   -0.8954   -2.5309 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3910   -1.2631   -1.9877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5406   -1.3493   -2.7439 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4347   -1.6044   -0.5606 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2641   -1.4793    0.1152 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7946   -0.2297    0.3909 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6617    0.0631   -0.3433 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3816    0.3064    0.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0312    0.2978    1.3276 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3582    0.5601    1.5851 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7663    0.5476    2.9317 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2596    0.8256    0.5741 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8867    0.8411   -0.7440 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7653    1.0350   -1.8641 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9980    0.7012   -1.9453 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7861    0.0314   -0.9587 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1411    0.3997   -0.9055 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0685   -0.2293   -0.1221 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6526   -1.2917    0.6663 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5481   -1.9570    1.4735 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3304   -1.6551    0.6159 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3905   -1.0346   -0.1652 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5266    0.5708   -0.9715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8712    0.8076    0.3068 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5542    1.9652    1.0156 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1135    0.2354    0.9783 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.0828    1.1997    1.1702 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6019   -0.9105    0.1025 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4130   -1.7970    0.8040 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0740   -0.5325   -3.0240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7005   -2.7069   -0.5272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4897   -0.2454    1.4852 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6547    0.0907    2.1646 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0972   -0.2651    3.3988 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2695    1.0723    0.8965 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2758    1.5477   -2.7627 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5188    0.9695   -2.9219 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4804    1.2255   -1.5137 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0946    0.0890   -0.1144 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5155   -1.7093    1.5258 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0308   -2.4896    1.2423 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3800   -1.3901   -0.2044 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2355    0.5870   -2.0302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1329    1.0004   -0.7315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6268    2.2610    0.8547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7731   -0.2186    1.9321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1341    1.4794    2.1313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2187   -0.4563   -0.6951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1682   -2.7319    0.6564 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 10 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
 13 23  2  0
  6 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 28  4  1  0
 23  8  1  0
 22 16  1  0
  3 30  1  0
  4 31  1  6
  6 32  1  1
  9 33  1  0
 11 34  1  0
 12 35  1  0
 14 36  1  0
 15 37  1  0
 17 38  1  0
 18 39  1  0
 20 40  1  0
 21 41  1  0
 22 42  1  0
 23 43  1  0
 24 44  1  6
 25 45  1  0
 26 46  1  1
 27 47  1  0
 28 48  1  6
 29 49  1  0
M  END


  Mrv0541 02271201282D          

 29 31  0  0  0  0            999 V2000
   -2.5377    0.7662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5377   -0.0588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2522   -0.4713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9667   -0.0588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9667    0.7662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2522    1.1787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2522    2.0037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9667    2.4162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6811   -0.4713    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8232   -0.4713    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6811    2.0037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3956    0.7662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1101    1.1787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1101    2.0037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3956    2.4162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6811    1.1787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8245    0.7662    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5377   -1.7088    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5377   -2.5338    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8232   -2.9463    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1087   -2.5338    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1088   -1.7088    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8232   -1.2963    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3943   -1.2963    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3943   -2.9463    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8232   -3.7713    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2522   -2.9463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2522   -3.7713    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9666   -2.5339    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  4  9  1  0  0  0  0
  2 10  1  0  0  0  0
  8 11  1  0  0  0  0
 15 11  2  0  0  0  0
 11 16  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 12 16  2  0  0  0  0
 13 17  1  0  0  0  0
 23 10  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 18 23  1  0  0  0  0
 22 24  1  6  0  0  0
 21 25  1  1  0  0  0
 20 26  1  6  0  0  0
 19 27  1  1  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0041711

> <DATABASE_NAME>
hmdb

> <SMILES>
O[C@H]1[C@H](OC2=CC(\C=C/C3=CC=C(O)C=C3)=CC(O)=C2)O[C@@H]([C@@H](O)[C@@H]1O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H20O9/c21-12-5-3-10(4-6-12)1-2-11-7-13(22)9-14(8-11)28-20-17(25)15(23)16(24)18(29-20)19(26)27/h1-9,15-18,20-25H,(H,26,27)/b2-1-/t15-,16-,17+,18-,20+/m0/s1

> <INCHI_KEY>
QWSAYEBSTMCFKY-BMPGWQKJSA-N

> <FORMULA>
C20H20O9

> <MOLECULAR_WEIGHT>
404.3674

> <EXACT_MASS>
404.110732238

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_AVERAGE_POLARIZABILITY>
38.971251279813444

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-{3-hydroxy-5-[(Z)-2-(4-hydroxyphenyl)ethenyl]phenoxy}oxane-2-carboxylic acid

> <ALOGPS_LOGP>
1.31

> <JCHEM_LOGP>
1.4545973309999998

> <ALOGPS_LOGS>
-2.69

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.10200942018762

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.1353625575872637

> <JCHEM_PKA_STRONGEST_BASIC>
-3.686826771564462

> <JCHEM_POLAR_SURFACE_AREA>
156.91

> <JCHEM_REFRACTIVITY>
99.46729999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.29e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-{3-hydroxy-5-[(Z)-2-(4-hydroxyphenyl)ethenyl]phenoxy}oxane-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0041711
     RDKit          3D
cis-Resveratrol 3-O-glucuronide
 49 51  0  0  0  0  0  0  0  0999 V2000
   -3.3297   -0.8954   -2.5309 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3910   -1.2631   -1.9877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5406   -1.3493   -2.7439 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4347   -1.6044   -0.5606 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2641   -1.4793    0.1152 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7946   -0.2297    0.3909 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6617    0.0631   -0.3433 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3816    0.3064    0.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0312    0.2978    1.3276 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3582    0.5601    1.5851 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7663    0.5476    2.9317 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2596    0.8256    0.5741 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8867    0.8411   -0.7440 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7653    1.0350   -1.8641 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9980    0.7012   -1.9453 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7861    0.0314   -0.9587 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1411    0.3997   -0.9055 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0685   -0.2293   -0.1221 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6526   -1.2917    0.6663 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5481   -1.9570    1.4735 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3304   -1.6551    0.6159 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3905   -1.0346   -0.1652 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5266    0.5708   -0.9715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8712    0.8076    0.3068 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5542    1.9652    1.0156 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1135    0.2354    0.9783 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.0828    1.1997    1.1702 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6019   -0.9105    0.1025 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4130   -1.7970    0.8040 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0740   -0.5325   -3.0240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7005   -2.7069   -0.5272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4897   -0.2454    1.4852 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6547    0.0907    2.1646 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0972   -0.2651    3.3988 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2695    1.0723    0.8965 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2758    1.5477   -2.7627 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5188    0.9695   -2.9219 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4804    1.2255   -1.5137 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0946    0.0890   -0.1144 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5155   -1.7093    1.5258 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0308   -2.4896    1.2423 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3800   -1.3901   -0.2044 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2355    0.5870   -2.0302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1329    1.0004   -0.7315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6268    2.2610    0.8547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7731   -0.2186    1.9321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1341    1.4794    2.1313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2187   -0.4563   -0.6951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1682   -2.7319    0.6564 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 10 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
 13 23  2  0
  6 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 28  4  1  0
 23  8  1  0
 22 16  1  0
  3 30  1  0
  4 31  1  6
  6 32  1  1
  9 33  1  0
 11 34  1  0
 12 35  1  0
 14 36  1  0
 15 37  1  0
 17 38  1  0
 18 39  1  0
 20 40  1  0
 21 41  1  0
 22 42  1  0
 23 43  1  0
 24 44  1  6
 25 45  1  0
 26 46  1  1
 27 47  1  0
 28 48  1  6
 29 49  1  0
M  END

HEADER    PROTEIN                                 27-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-FEB-12         0                                  
HETATM    1  C   UNK     0      -4.737   1.430   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.737  -0.110   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -6.071  -0.880   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -7.405  -0.110   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -7.405   1.430   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -6.071   2.200   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.071   3.740   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -7.405   4.510   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -8.738  -0.880   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      -3.403  -0.880   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -8.738   3.740   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -10.072   1.430   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -11.406   2.200   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -11.406   3.740   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -10.072   4.510   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -8.738   2.200   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0     -12.739   1.430   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      -4.737  -3.190   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -4.737  -4.730   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -3.403  -5.500   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.070  -4.730   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.070  -3.190   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -3.403  -2.420   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.736  -2.420   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      -0.736  -5.500   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      -3.403  -7.040   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -6.071  -5.500   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -6.071  -7.040   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -7.404  -4.730   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   10                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    1    5    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7   11                                                       
CONECT    9    4                                                            
CONECT   10    2   23                                                       
CONECT   11    8   15   16                                                  
CONECT   12   13   16                                                       
CONECT   13   12   14   17                                                  
CONECT   14   13   15                                                       
CONECT   15   11   14                                                       
CONECT   16   11   12                                                       
CONECT   17   13                                                            
CONECT   18   19   23                                                       
CONECT   19   18   20   27                                                  
CONECT   20   19   21   26                                                  
CONECT   21   20   22   25                                                  
CONECT   22   21   23   24                                                  
CONECT   23   10   22   18                                                  
CONECT   24   22                                                            
CONECT   25   21                                                            
CONECT   26   20                                                            
CONECT   27   19   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

COMPND    HMDB0041711
HETATM    1  O1  UNL     1      -3.330  -0.895  -2.531  1.00  0.00           O  
HETATM    2  C1  UNL     1      -4.391  -1.263  -1.988  1.00  0.00           C  
HETATM    3  O2  UNL     1      -5.541  -1.349  -2.744  1.00  0.00           O  
HETATM    4  C2  UNL     1      -4.435  -1.604  -0.561  1.00  0.00           C  
HETATM    5  O3  UNL     1      -3.264  -1.479   0.115  1.00  0.00           O  
HETATM    6  C3  UNL     1      -2.795  -0.230   0.391  1.00  0.00           C  
HETATM    7  O4  UNL     1      -1.662   0.063  -0.343  1.00  0.00           O  
HETATM    8  C4  UNL     1      -0.382   0.306   0.022  1.00  0.00           C  
HETATM    9  C5  UNL     1       0.031   0.298   1.328  1.00  0.00           C  
HETATM   10  C6  UNL     1       1.358   0.560   1.585  1.00  0.00           C  
HETATM   11  O5  UNL     1       1.766   0.548   2.932  1.00  0.00           O  
HETATM   12  C7  UNL     1       2.260   0.826   0.574  1.00  0.00           C  
HETATM   13  C8  UNL     1       1.887   0.841  -0.744  1.00  0.00           C  
HETATM   14  C9  UNL     1       2.765   1.035  -1.864  1.00  0.00           C  
HETATM   15  C10 UNL     1       3.998   0.701  -1.945  1.00  0.00           C  
HETATM   16  C11 UNL     1       4.786   0.031  -0.959  1.00  0.00           C  
HETATM   17  C12 UNL     1       6.141   0.400  -0.906  1.00  0.00           C  
HETATM   18  C13 UNL     1       7.068  -0.229  -0.122  1.00  0.00           C  
HETATM   19  C14 UNL     1       6.653  -1.292   0.666  1.00  0.00           C  
HETATM   20  O6  UNL     1       7.548  -1.957   1.473  1.00  0.00           O  
HETATM   21  C15 UNL     1       5.330  -1.655   0.616  1.00  0.00           C  
HETATM   22  C16 UNL     1       4.391  -1.035  -0.165  1.00  0.00           C  
HETATM   23  C17 UNL     1       0.527   0.571  -0.971  1.00  0.00           C  
HETATM   24  C18 UNL     1      -3.871   0.808   0.307  1.00  0.00           C  
HETATM   25  O7  UNL     1      -3.554   1.965   1.016  1.00  0.00           O  
HETATM   26  C19 UNL     1      -5.113   0.235   0.978  1.00  0.00           C  
HETATM   27  O8  UNL     1      -6.083   1.200   1.170  1.00  0.00           O  
HETATM   28  C20 UNL     1      -5.602  -0.910   0.103  1.00  0.00           C  
HETATM   29  O9  UNL     1      -6.413  -1.797   0.804  1.00  0.00           O  
HETATM   30  H1  UNL     1      -6.074  -0.533  -3.024  1.00  0.00           H  
HETATM   31  H2  UNL     1      -4.700  -2.707  -0.527  1.00  0.00           H  
HETATM   32  H3  UNL     1      -2.490  -0.245   1.485  1.00  0.00           H  
HETATM   33  H4  UNL     1      -0.655   0.091   2.165  1.00  0.00           H  
HETATM   34  H5  UNL     1       2.097  -0.265   3.399  1.00  0.00           H  
HETATM   35  H6  UNL     1       3.269   1.072   0.897  1.00  0.00           H  
HETATM   36  H7  UNL     1       2.276   1.548  -2.763  1.00  0.00           H  
HETATM   37  H8  UNL     1       4.519   0.969  -2.922  1.00  0.00           H  
HETATM   38  H9  UNL     1       6.480   1.226  -1.514  1.00  0.00           H  
HETATM   39  H10 UNL     1       8.095   0.089  -0.114  1.00  0.00           H  
HETATM   40  H11 UNL     1       8.516  -1.709   1.526  1.00  0.00           H  
HETATM   41  H12 UNL     1       5.031  -2.490   1.242  1.00  0.00           H  
HETATM   42  H13 UNL     1       3.380  -1.390  -0.204  1.00  0.00           H  
HETATM   43  H14 UNL     1       0.236   0.587  -2.030  1.00  0.00           H  
HETATM   44  H15 UNL     1      -4.133   1.000  -0.731  1.00  0.00           H  
HETATM   45  H16 UNL     1      -2.627   2.261   0.855  1.00  0.00           H  
HETATM   46  H17 UNL     1      -4.773  -0.219   1.932  1.00  0.00           H  
HETATM   47  H18 UNL     1      -6.134   1.479   2.131  1.00  0.00           H  
HETATM   48  H19 UNL     1      -6.219  -0.456  -0.695  1.00  0.00           H  
HETATM   49  H20 UNL     1      -6.168  -2.732   0.656  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3    4
CONECT    3   30
CONECT    4    5   28   31
CONECT    5    6
CONECT    6    7   24   32
CONECT    7    8
CONECT    8    9    9   23
CONECT    9   10   33
CONECT   10   11   12   12
CONECT   11   34
CONECT   12   13   35
CONECT   13   14   23   23
CONECT   14   15   15   36
CONECT   15   16   37
CONECT   16   17   17   22
CONECT   17   18   38
CONECT   18   19   19   39
CONECT   19   20   21
CONECT   20   40
CONECT   21   22   22   41
CONECT   22   42
CONECT   23   43
CONECT   24   25   26   44
CONECT   25   45
CONECT   26   27   28   46
CONECT   27   47
CONECT   28   29   48
CONECT   29   49
END

HMDB0041711
     RDKit          3D
cis-Resveratrol 3-O-glucuronide
 49 51  0  0  0  0  0  0  0  0999 V2000
   -3.3297   -0.8954   -2.5309 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3910   -1.2631   -1.9877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5406   -1.3493   -2.7439 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4347   -1.6044   -0.5606 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2641   -1.4793    0.1152 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7946   -0.2297    0.3909 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6617    0.0631   -0.3433 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3816    0.3064    0.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0312    0.2978    1.3276 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3582    0.5601    1.5851 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7663    0.5476    2.9317 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2596    0.8256    0.5741 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8867    0.8411   -0.7440 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7653    1.0350   -1.8641 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9980    0.7012   -1.9453 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7861    0.0314   -0.9587 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1411    0.3997   -0.9055 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0685   -0.2293   -0.1221 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6526   -1.2917    0.6663 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5481   -1.9570    1.4735 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3304   -1.6551    0.6159 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3905   -1.0346   -0.1652 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5266    0.5708   -0.9715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8712    0.8076    0.3068 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5542    1.9652    1.0156 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1135    0.2354    0.9783 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.0828    1.1997    1.1702 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6019   -0.9105    0.1025 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4130   -1.7970    0.8040 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0740   -0.5325   -3.0240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7005   -2.7069   -0.5272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4897   -0.2454    1.4852 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6547    0.0907    2.1646 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0972   -0.2651    3.3988 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2695    1.0723    0.8965 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2758    1.5477   -2.7627 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5188    0.9695   -2.9219 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4804    1.2255   -1.5137 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0946    0.0890   -0.1144 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5155   -1.7093    1.5258 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0308   -2.4896    1.2423 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3800   -1.3901   -0.2044 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2355    0.5870   -2.0302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1329    1.0004   -0.7315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6268    2.2610    0.8547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7731   -0.2186    1.9321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1341    1.4794    2.1313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2187   -0.4563   -0.6951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1682   -2.7319    0.6564 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 10 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
 13 23  2  0
  6 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 28  4  1  0
 23  8  1  0
 22 16  1  0
  3 30  1  0
  4 31  1  6
  6 32  1  1
  9 33  1  0
 11 34  1  0
 12 35  1  0
 14 36  1  0
 15 37  1  0
 17 38  1  0
 18 39  1  0
 20 40  1  0
 21 41  1  0
 22 42  1  0
 23 43  1  0
 24 44  1  6
 25 45  1  0
 26 46  1  1
 27 47  1  0
 28 48  1  6
 29 49  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₀H₂₀O₉

Average Molecular Weight

404.3674

Monoisotopic Molecular Weight

404.110732238

IUPAC Name

(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-{3-hydroxy-5-[(Z)-2-(4-hydroxyphenyl)ethenyl]phenoxy}oxane-2-carboxylic acid

Traditional Name

(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-{3-hydroxy-5-[(Z)-2-(4-hydroxyphenyl)ethenyl]phenoxy}oxane-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

O[C@H]1[C@H](OC2=CC(\C=C/C3=CC=C(O)C=C3)=CC(O)=C2)O[C@@H]([C@@H](O)[C@@H]1O)C(O)=O

InChI Identifier

InChI=1S/C20H20O9/c21-12-5-3-10(4-6-12)1-2-11-7-13(22)9-14(8-11)28-20-17(25)15(23)16(24)18(29-20)19(26)27/h1-9,15-18,20-25H,(H,26,27)/b2-1-/t15-,16-,17+,18-,20+/m0/s1

InChI Key

QWSAYEBSTMCFKY-BMPGWQKJSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as stilbene glycosides. Stilbene glycosides are compounds structurally characterized by the presence of a carbohydrate moiety glycosidically linked to the stilbene skeleton.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Stilbenes

Sub Class

Stilbene glycosides

Direct Parent

Stilbene glycosides

Alternative Parents

Substituents

Stilbene glycoside
Phenolic glycoside
1-o-glucuronide
O-glucuronide
Glucuronic acid or derivatives
Glycosyl compound
O-glycosyl compound
Phenoxy compound
Styrene
Phenol ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Beta-hydroxy acid
Phenol
Monocyclic benzene moiety
Hydroxy acid
Monosaccharide
Benzenoid
Oxane
Pyran
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Acetal
Polyol
Alcohol
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organic oxygen compound
Carbonyl group
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

beta-D-glucosiduronic acid (CHEBI:86971 )
stilbenol (CHEBI:86971 )

Ontology

Not Available

Blood (HMDB: HMDB0041711)
Urine (HMDB: HMDB0041711)

Organ

Liver (HMDB: HMDB0041711)
Kidney (HMDB: HMDB0041711)

Excreta

Biofluid or Excreta

Urine (PMID: 17170057)

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 32966057)

Cellular substructure

Extracellular (HMDB: HMDB0041711)
Cytoplasm (HMDB: HMDB0041711)

Source

Endogenous

Endogenous (HMDB: HMDB0041711)

Plant

Plant (HMDB: HMDB0041711)

Exogenous

Food

Food (HMDB: HMDB0041711)

Beverage

Alcoholic beverage

Red wine (HMDB: HMDB0041711)

Fruit

Grapes (HMDB: HMDB0041711)

Not Available

Nutrient (HMDB: HMDB0041711)

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.83 g/L	ALOGPS
logP	1.31	ALOGPS
logP	1.45	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	3.14	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	156.91 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	99.47 m³·mol⁻¹	ChemAxon
Polarizability	38.97 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	197.173	30932474
DeepCCS	[M-H]-	194.531	30932474
DeepCCS	[M-2H]-	228.129	30932474
DeepCCS	[M+Na]+	204.49	30932474
AllCCS	[M+H]+	195.7	32859911
AllCCS	[M+H-H2O]+	193.0	32859911
AllCCS	[M+NH4]+	198.2	32859911
AllCCS	[M+Na]+	198.9	32859911
AllCCS	[M-H]-	191.3	32859911
AllCCS	[M+Na-2H]-	191.5	32859911
AllCCS	[M+HCOO]-	191.8	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
cis-Resveratrol 3-O-glucuronide	O[C@H]1[C@H](OC2=CC(\C=C/C3=CC=C(O)C=C3)=CC(O)=C2)O[C@@H]([C@@H](O)[C@@H]1O)C(O)=O	6292.0	Standard polar	33892256
cis-Resveratrol 3-O-glucuronide	O[C@H]1[C@H](OC2=CC(\C=C/C3=CC=C(O)C=C3)=CC(O)=C2)O[C@@H]([C@@H](O)[C@@H]1O)C(O)=O	4011.8	Standard non polar	33892256
cis-Resveratrol 3-O-glucuronide	O[C@H]1[C@H](OC2=CC(\C=C/C3=CC=C(O)C=C3)=CC(O)=C2)O[C@@H]([C@@H](O)[C@@H]1O)C(O)=O	4153.3	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
cis-Resveratrol 3-O-glucuronide,1TMS,isomer #1	C[Si](C)(C)O[C@H]1[C@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)O[C@H](C(=O)O)[C@@H](O)[C@@H]1O	3849.4	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,1TMS,isomer #2	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]3O)=C2)C=C1	3846.0	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,1TMS,isomer #3	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)=C1	3824.5	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,1TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)[C@H](O)[C@H]1O	3849.9	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,1TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)O[C@H](C(=O)O)[C@H]1O	3831.9	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,1TMS,isomer #6	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)[C@H](O)[C@@H](O)[C@@H]1O	3836.9	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TMS,isomer #1	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=C1	3771.2	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TMS,isomer #10	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O)C=C3)=CC(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O	3787.5	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TMS,isomer #11	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=C1	3770.8	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TMS,isomer #12	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=C1	3751.1	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TMS,isomer #13	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3814.2	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TMS,isomer #14	C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)[C@H](O)[C@H]1O[Si](C)(C)C	3818.4	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TMS,isomer #15	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3797.8	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TMS,isomer #2	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)=C2)C=C1	3802.0	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TMS,isomer #3	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3809.3	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)[C@H](O[Si](C)(C)C)[C@H]1O	3826.9	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TMS,isomer #5	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](C(=O)O)O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)[C@@H]1O[Si](C)(C)C	3805.1	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TMS,isomer #6	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]3O)=CC(O[Si](C)(C)C)=C2)C=C1	3825.3	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TMS,isomer #7	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O[Si](C)(C)C)C=C3)=C2)[C@H](O)[C@@H](O)[C@@H]1O	3805.4	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TMS,isomer #8	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)=C2)C=C1	3796.8	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TMS,isomer #9	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)=C2)C=C1	3776.4	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TMS,isomer #1	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1	3778.2	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TMS,isomer #10	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)O[C@H](C(=O)O)[C@H]1O[Si](C)(C)C	3764.3	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TMS,isomer #11	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O[Si](C)(C)C)C=C3)=CC(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O	3776.6	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TMS,isomer #12	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)=CC(O[Si](C)(C)C)=C2)C=C1	3776.5	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TMS,isomer #13	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)=CC(O[Si](C)(C)C)=C2)C=C1	3765.3	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TMS,isomer #14	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O[Si](C)(C)C)C=C3)=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3717.4	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TMS,isomer #15	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O[Si](C)(C)C)C=C3)=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3761.4	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TMS,isomer #16	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)=C2)C=C1	3749.2	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TMS,isomer #17	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O)C=C3)=CC(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3716.7	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TMS,isomer #18	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O)C=C3)=CC(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3763.6	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TMS,isomer #19	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)=C1	3739.6	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TMS,isomer #2	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O)C=C3)=CC(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3748.3	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TMS,isomer #20	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3765.7	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TMS,isomer #3	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)=C1	3744.9	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TMS,isomer #4	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=C1	3725.8	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TMS,isomer #5	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O[Si](C)(C)C)C=C3)=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3754.0	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TMS,isomer #6	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)=C2)C=C1	3758.6	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TMS,isomer #7	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C2)C=C1	3740.1	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TMS,isomer #8	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3754.9	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TMS,isomer #9	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3780.2	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TMS,isomer #1	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O[Si](C)(C)C)C=C3)=CC(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3747.9	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TMS,isomer #10	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3760.0	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TMS,isomer #11	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O[Si](C)(C)C)C=C3)=CC(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3743.2	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TMS,isomer #12	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O[Si](C)(C)C)C=C3)=CC(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3759.1	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TMS,isomer #13	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)=CC(O[Si](C)(C)C)=C2)C=C1	3754.4	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TMS,isomer #14	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O[Si](C)(C)C)C=C3)=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3706.0	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TMS,isomer #15	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O)C=C3)=CC(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3711.3	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TMS,isomer #2	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1	3758.5	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TMS,isomer #3	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1	3746.7	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TMS,isomer #4	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O)C=C3)=CC(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3696.5	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TMS,isomer #5	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O)C=C3)=CC(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3718.5	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TMS,isomer #6	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=C1	3718.5	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TMS,isomer #7	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O[Si](C)(C)C)C=C3)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3701.7	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TMS,isomer #8	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O[Si](C)(C)C)C=C3)=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3721.7	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TMS,isomer #9	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C2)C=C1	3723.7	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,5TMS,isomer #1	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O[Si](C)(C)C)C=C3)=CC(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3743.2	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,5TMS,isomer #2	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O[Si](C)(C)C)C=C3)=CC(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3757.3	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,5TMS,isomer #3	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1	3747.3	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,5TMS,isomer #4	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O)C=C3)=CC(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3712.2	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,5TMS,isomer #5	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O[Si](C)(C)C)C=C3)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3714.9	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,5TMS,isomer #6	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O[Si](C)(C)C)C=C3)=CC(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3744.8	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,6TMS,isomer #1	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O[Si](C)(C)C)C=C3)=CC(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3765.0	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)O[C@H](C(=O)O)[C@@H](O)[C@@H]1O	4098.0	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]3O)=C2)C=C1	4124.2	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)=C1	4098.7	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)[C@H](O)[C@H]1O	4091.1	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)O[C@H](C(=O)O)[C@H]1O	4085.9	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)[C@H](O)[C@@H](O)[C@@H]1O	4131.8	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)=C1	4272.9	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O)C=C3)=CC(O[Si](C)(C)C(C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O	4299.0	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)=C1	4256.3	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)=C1	4249.5	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4294.8	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4240.6	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4272.0	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)=C2)C=C1	4293.8	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	4287.9	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4254.0	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](C(=O)O)O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)[C@@H]1O[Si](C)(C)C(C)(C)C	4238.8	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1	4351.5	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)=C2)[C@H](O)[C@@H](O)[C@@H]1O	4312.6	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)=C2)C=C1	4275.8	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)=C2)C=C1	4264.2	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1	4546.9	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)O[C@H](C(=O)O)[C@H]1O[Si](C)(C)C(C)(C)C	4394.5	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)=CC(O[Si](C)(C)C(C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O	4548.1	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1	4537.1	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1	4548.6	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)=C2)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4447.4	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4481.4	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)=C2)C=C1	4435.7	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O)C=C3)=CC(O[Si](C)(C)C(C)(C)C)=C2)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4450.3	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O)C=C3)=CC(O[Si](C)(C)C(C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4479.1	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)=C1	4428.6	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O)C=C3)=CC(O[Si](C)(C)C(C)(C)C)=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	4466.9	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	4430.7	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)=C1	4435.2	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)=C1	4425.0	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	4473.7	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)=C2)C=C1	4446.5	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)=C2)C=C1	4432.6	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4413.5	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4449.3	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)=CC(O[Si](C)(C)C(C)(C)C)=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	4712.0	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	4571.9	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)=CC(O[Si](C)(C)C(C)(C)C)=C2)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4709.2	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)=CC(O[Si](C)(C)C(C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4714.3	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1	4694.1	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)=C2)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	4588.3	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O)C=C3)=CC(O[Si](C)(C)C(C)(C)C)=C2)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	4589.9	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1	4701.5	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1	4690.3	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O)C=C3)=CC(O[Si](C)(C)C(C)(C)C)=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4585.4	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(/C=C\C3=CC=C(O)C=C3)=CC(O[Si](C)(C)C(C)(C)C)=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4614.2	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)=C1	4578.8	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4583.0	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=CC(/C=C\C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4614.8	Semi standard non polar	33892256
cis-Resveratrol 3-O-glucuronide,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)=C2)C=C1	4596.6	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Resveratrol 3-O-glucuronide GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a4u-9145000000-699b35990650560051b5	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Resveratrol 3-O-glucuronide GC-MS (4 TMS) - 70eV, Positive	splash10-004i-3502019000-9a6f87ff263731d65b7c	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Resveratrol 3-O-glucuronide GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Resveratrol 3-O-glucuronide GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Resveratrol 3-O-glucuronide 10V, Positive-QTOF	splash10-0570-0194200000-cb4bbb4daab2cd819ebd	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Resveratrol 3-O-glucuronide 20V, Positive-QTOF	splash10-004i-0590000000-9dfd444bbf39f5b59bf5	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Resveratrol 3-O-glucuronide 40V, Positive-QTOF	splash10-0c29-1930000000-47fcf0acd4ddeb9fc9f0	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Resveratrol 3-O-glucuronide 10V, Negative-QTOF	splash10-0zi0-1296800000-1c9b18e9d229b79c7b25	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Resveratrol 3-O-glucuronide 20V, Negative-QTOF	splash10-004i-1292000000-9ed0bfa85e67333138a1	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Resveratrol 3-O-glucuronide 40V, Negative-QTOF	splash10-004i-4690000000-4d7698c9a1ab3b1f11f3	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Resveratrol 3-O-glucuronide 10V, Positive-QTOF	splash10-056r-0190300000-b002575baf270824a927	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Resveratrol 3-O-glucuronide 20V, Positive-QTOF	splash10-004i-0691100000-2cc7d9dfd8625886170c	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Resveratrol 3-O-glucuronide 40V, Positive-QTOF	splash10-01t9-3960000000-14c30accf234596ea71d	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Resveratrol 3-O-glucuronide 10V, Negative-QTOF	splash10-004i-0090100000-b08f62a84c353beb8d3d	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Resveratrol 3-O-glucuronide 20V, Negative-QTOF	splash10-004i-0290000000-d4e0babb1dda3df7caa6	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Resveratrol 3-O-glucuronide 40V, Negative-QTOF	splash10-0059-1960000000-968c14c839d9f0c4d948	2021-09-23	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm
Extracellular

Biospecimen Locations

Blood
Urine

Tissue Locations

Kidney
Liver

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Expected but not Quantified	Not Quantified	Not Available	Not Available	Normal	Not Available	details
Blood	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Normal	32966057	details
Urine	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Normal	32966057	details
Urine	Expected but not Quantified	Not Quantified	Not Available	Not Available	Consuming polyphenols described by Phenol-Explorer entry 995	17170057	details
Urine	Expected but not Quantified	Not Quantified	Not Available	Not Available	Consuming polyphenols described by Phenol-Explorer entry 995	16675507	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB029877

KNApSAcK ID

Not Available

Chemspider ID

30777610

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

29986850

PDB ID

Not Available

ChEBI ID

86971

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Neveu V, Perez-Jimenez J, Vos F, Crespy V, du Chaffaut L, Mennen L, Knox C, Eisner R, Cruz J, Wishart D, Scalbert A: Phenol-Explorer: an online comprehensive database on polyphenol contents in foods. Database (Oxford). 2010;2010:bap024. doi: 10.1093/database/bap024. Epub 2010 Jan 8. [PubMed:20428313 ]

Showing metabocard for cis-Resveratrol 3-O-glucuronide (HMDB0041711)

MOL for HMDB0041711 (cis-Resveratrol 3-O-glucuronide)

3D MOL for HMDB0041711 (cis-Resveratrol 3-O-glucuronide)

3D SDF for HMDB0041711 (cis-Resveratrol 3-O-glucuronide)

3D-SDF for HMDB0041711 (cis-Resveratrol 3-O-glucuronide)

PDB for HMDB0041711 (cis-Resveratrol 3-O-glucuronide)

3D PDB for HMDB0041711 (cis-Resveratrol 3-O-glucuronide)

SMILES for HMDB0041711 (cis-Resveratrol 3-O-glucuronide)

INCHI for HMDB0041711 (cis-Resveratrol 3-O-glucuronide)

Structure for HMDB0041711 (cis-Resveratrol 3-O-glucuronide)

3D Structure for HMDB0041711 (cis-Resveratrol 3-O-glucuronide)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra